A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3735n54



Internal ID20137159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66962955..66989369hg38UCSC Ensembl
chr14:67429672..67456086hg19UCSC Ensembl
chr14:66499425..66525839hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3826415
hg1926415
hg1826415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564959, nsv564958
Samples
Known GenesGPHN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3735n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer